Volume 24, Issue 14
Heterocyclic Compounds
Full Access

ChemInform Abstract: Diastereo- and Enantioselective Synthesis of trans-3-Phenyl- and trans- 3-Styryl-2-azetidinones via Zinc Ester Enolates and Imines.

H. KLEIJN

H. KLEIJN

Dep. Met.-Mediated Synth., Utrecht Univ., 3584 CH Utrecht, Neth.

Search for more papers by this author
H. L. VAN MAANEN

H. L. VAN MAANEN

Dep. Met.-Mediated Synth., Utrecht Univ., 3584 CH Utrecht, Neth.

Search for more papers by this author
J. T. B. H. JASTRZEBSKI

J. T. B. H. JASTRZEBSKI

Dep. Met.-Mediated Synth., Utrecht Univ., 3584 CH Utrecht, Neth.

Search for more papers by this author
G. VAN KOTEN

G. VAN KOTEN

Dep. Met.-Mediated Synth., Utrecht Univ., 3584 CH Utrecht, Neth.

Search for more papers by this author
First published: April 6, 1993

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

ChemInform Abstract

Zn enolates of phenyl- and trans-styryl-acetic acid methyl ester (I) react with excellent diastereoselectivity and good enantioselectivity ( 64 to 91.5% e.e.) with imines such as (II) and (V) to give the title compounds, e.g. (III) and (V). The corresponding Li enolates react with much lower selectivity and yields.

chemical structure image

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.